Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 4308
Gene Symbol: TRPM1
TRPM1 		0.600 GeneticVariation disease CLINVAR Whole Genome Sequencing Increases Molecular Diagnostic Yield Compared with Current Diagnostic Testing for Inherited Retinal Disease. 26872967 2016
Entrez Id: 4308
Gene Symbol: TRPM1
TRPM1 		0.600 GeneticVariation disease CLINVAR TRPM1 mutations are associated with the complete form of congenital stationary night blindness. 20300565 2010
Entrez Id: 4308
Gene Symbol: TRPM1
TRPM1 		0.600 GeneticVariation disease CLINVAR TRPM1 is mutated in patients with autosomal-recessive complete congenital stationary night blindness. 19896113 2009
Entrez Id: 4308
Gene Symbol: TRPM1
TRPM1 		0.600 GeneticVariation disease UNIPROT TRPM1 is mutated in patients with autosomal-recessive complete congenital stationary night blindness. 19896113 2009
Entrez Id: 4308
Gene Symbol: TRPM1
TRPM1 		0.600 Biomarker disease GENOMICS_ENGLAND TRPM1 is mutated in patients with autosomal-recessive complete congenital stationary night blindness. 19896113 2009
Entrez Id: 4308
Gene Symbol: TRPM1
TRPM1 		0.600 GeneticVariation disease UNIPROT Mutations in TRPM1 are a common cause of complete congenital stationary night blindness. 19896109 2009
Entrez Id: 4308
Gene Symbol: TRPM1
TRPM1 		0.600 GeneticVariation disease UNIPROT Recessive mutations of the gene TRPM1 abrogate ON bipolar cell function and cause complete congenital stationary night blindness in humans. 19878917 2009
Entrez Id: 4308
Gene Symbol: TRPM1
TRPM1 		0.600 CausalMutation disease CLINVAR
Entrez Id: 4308
Gene Symbol: TRPM1
TRPM1 		0.600 Biomarker disease GENOMICS_ENGLAND